Browsing by Subject Mutation
Showing results 1 to 2 of 2
Issue Date | Title | Author(s) |
---|---|---|
1996 | Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene. | Booth, David R.; Tan, Si-Yen; Booth, Sussanne E.; Tennent, Glenys A.; Hutchinson, Winston L.; Hsuan, J. Justin; Totty, Nicholas F.; Truong, Oanh; Soutar, Anne K.; Hawkins, Philip N.; Bruguera i Cortada, Miquel, 1942-; Caballeria Rovira, Joan; Solé, Manel; Campistol Plana, Josep M.; Pepys, Mark B. |
6-Jul-2023 | The Prognostic Significance of Tumor-Infiltrating Lymphocytes, PD-L1, BRCA Mutation Status and Tumor Mutational Burden in Early-Stage High-Grade Serous Ovarian Carcinoma—A Study by the Spanish Group for Ovarian Cancer Research (GEICO) | Pizarro, David; Romero, Ignacio; Pérez Mies, Belén; Redondo, Andrés; Caniego Casas, Tamara; Carretero Barrio, Irene; Cristóbal, Eva; Gutiérrez Pecharromán, Ana; Santaballa, Ana; D’angelo, Emanuela; Hardisson, David; Vieites, Begoña; Matías Guiu, Xavier; Estévez, Purificación; Guerra, Eva; Prat, Jaime; Poveda, Andrés; López Guerrero, José Antonio; Palacios, José |